Canonical Allele Identifier: CA350472998

Gene: ATIC

Linked Data

• MyVariant Identifiers: chr2:g.215325196_215325197del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215325196_215325197del , CM000664.2:g.215325196_215325197del	GRCh38
NC_000002.11:g.216189919_216189920del , CM000664.1:g.216189919_216189920del	GRCh37
NC_000002.10:g.215898164_215898165del	NCBI36
NG_013002.1:g.18241_18242del

Transcript Alleles

HGVS	Amino-acid change
ENST00000236959.14:c.291-45_291-44del MANE Select	ENSP00000236959.9:n.291-45_291-44del
ENST00000236959.13:c.291-45_291-44del	ENSP00000236959.9:n.291-45_291-44del
ENST00000413174.1:c.114-45_114-44del	ENSP00000402393.1:n.114-45_114-44del
ENST00000427397.5:c.*341-45_*341-44del	ENSP00000394317.1:n.*341-45_*341-44del
ENST00000435675.5:c.288-45_288-44del	ENSP00000415935.1:n.288-45_288-44del
ENST00000443953.5:c.*388-45_*388-44del	ENSP00000406792.1:n.*388-45_*388-44del
ENST00000444305.5:c.224-45_224-44del	ENSP00000388675.1:n.224-45_224-44del
ENST00000488712.5:n.458_459del
NM_004044.6:c.291-45_291-44del	NP_004035.2:n.291-45_291-44del
XM_017004187.2:c.291-45_291-44del	XP_016859676.1:n.291-45_291-44del
XM_024452919.1:c.114-45_114-44del	XP_024308687.1:n.114-45_114-44del
NM_004044.7:c.291-45_291-44del MANE Select	NP_004035.2:n.291-45_291-44del